| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28349015-28349178 | Common:2; Rare:47 | ||||
| chr3:29280894-29281081 | Common:2; Rare:35 | ||||
| chr3:31981625-31981808 | Common:1; Rare:49 | ||||
| chr3:32238548-32238678 | Common:1; Rare:47 | ||||
| chr3:32502779-32503059 | Rare:61 | ||||
| chr3:32570366-32570900 | Common:1; Rare:208 | ||||
| chr3:33798520-33798719 | Common:2; Rare:73 | ||||
| chr3:33799014-33799194 | Rare:59 | ||||
| chr3:36993108-36993550 | Common:2; Rare:139; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr3:37176104-37176383 | Common:1; Rare:74 | ||||
| chr3:37243025-37243392 | Common:5; Rare:97 | ||||
| chr3:37861719-37861920 | Common:1; Rare:45 | ||||
| chr3:38024453-38024657 | Common:1; Rare:77 | ||||
| chr3:39051944-39052042 | Common:1; Rare:35 | ||||
| chr3:39107561-39107730 | Common:4; Rare:54 |